drugset / Trial / NCT00267748

Sunitinib Malate Schedule 4/2 vs. Sunitinib Malate Continuous Dosing As First-Line Therapy For Metastatic Renal Cell Cancer (RCC)

NCT00267748 ↗

Phase 2 Completed 317 enrolled Pfizer
RandomizedParallel-groupOpen-labelTreatment

Summary

This trial has two parts. The purpose of the first part of the trial is to determine the doses of 2 drugs, sunitinib malate and interferon alfa-2b, that can be given safely in combination. This part is currently closed to enrollment. The purpose of the second part of the trial is to see if sunitinib malate given on a 4/2 schedule (4 weeks on treatment, 2 weeks off treatment cycle) is any better at delaying progression of renal cell cancer than sunitinib malate given on a continuous dosing schedule. The trial will also determine the number of patients whose cancer responds to the treatments, whether life of patients can be extended, what the side effects are of the treatments, how bothersome disease or treatment-related symptoms are to patients, and whether tests can be found that will predict which patients may or may not respond to these treatments in the future.

Timeline

Start
2005-12
Primary completion
2010-06
Completion
2010-06

Outcome

Missed primary endpoint

registry Sunitinib 50 mg (Schedule 4/2) vs Sunitinib 37.5 mg; p = 0.220; Hazard Ratio (HR) 0.827 (95% CI 0.609 to 1.124) NCT00267748 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Sunitinib Small molecule 37.5 mg —
Subject Sunitinib Small molecule 50 mg —

Indications